Reacción #84130

Ecuación de reacción

benzylmethylamine

6-chloro-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

sodium tert-butoxide

2,4 di-tert-butylphosphino-2′,4′,6′-triisopropyl biphenyl

→

benzyl-methyl-(2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indol-6-yl)-amine

Rendimiento 109.1%

Disolventes

toluene

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.STIRRINGis stirred at 100° C. for 16 h
2. 2
   FiltraciónThe reaction mixture is filtered
3. 3
   Lavadothe residue washed with EtOAc
4. 4
   ConcentraciónThe filtrate is concentrated under reduced pressure
5. 5
   Otroto afford crude material, which
6. 6
   Otrois purified by reverse phase HPLC

Procedimiento

To a degassed mixture of 6-chloro-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (2-B) (100 mg, 0.5 mmol), sodium tert-butoxide (576 mg, 6.0 mmol), palladium acetate (22.4 mg, 0.1 mmol) and 2,4 di-tert-butylphosphino-2′,4′,6′-triisopropyl biphenyl (63.0 mg, 0.15 mmol) is added dry toluene (2 mL). After stirring for 5 min, benzylmethylamine (0.09 mL, 0.7 mmol) is added to the reaction mixture, which is stirred at 100° C. for 16 h. The reaction mixture is filtered and the residue washed with EtOAc. The filtrate is concentrated under reduced pressure to afford crude material, which is purified by reverse phase HPLC to yield benzyl-methyl-(2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indol-6-yl)-amine (2-C) (50 mg).

Fuente